Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 4 |
NetGPI | no | yes: 0, no: 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QCB0
Term | Name | Level | Count |
---|---|---|---|
GO:0007015 | actin filament organization | 5 | 5 |
GO:0007165 | signal transduction | 2 | 2 |
GO:0009987 | cellular process | 1 | 5 |
GO:0016043 | cellular component organization | 3 | 5 |
GO:0019932 | second-messenger-mediated signaling | 4 | 2 |
GO:0019933 | cAMP-mediated signaling | 6 | 2 |
GO:0019935 | cyclic-nucleotide-mediated signaling | 5 | 2 |
GO:0031279 | regulation of cyclase activity | 4 | 2 |
GO:0035556 | intracellular signal transduction | 3 | 2 |
GO:0045761 | regulation of adenylate cyclase activity | 5 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050790 | regulation of catalytic activity | 3 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051339 | regulation of lyase activity | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0065009 | regulation of molecular function | 2 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 5 |
GO:0097435 | supramolecular fiber organization | 4 | 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003779 | actin binding | 4 | 5 |
GO:0005488 | binding | 1 | 5 |
GO:0005515 | protein binding | 2 | 5 |
GO:0008092 | cytoskeletal protein binding | 3 | 5 |
GO:0008179 | adenylate cyclase binding | 4 | 2 |
GO:0019899 | enzyme binding | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 576 | 580 | PF00656 | 0.495 |
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.617 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 470 | 472 | PF00675 | 0.750 |
CLV_NRD_NRD_1 | 481 | 483 | PF00675 | 0.731 |
CLV_PCSK_FUR_1 | 244 | 248 | PF00082 | 0.593 |
CLV_PCSK_FUR_1 | 251 | 255 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 470 | 472 | PF00082 | 0.750 |
CLV_PCSK_KEX2_1 | 481 | 483 | PF00082 | 0.731 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.625 |
CLV_PCSK_SKI1_1 | 418 | 422 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 56 | 60 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 706 | 710 | PF00082 | 0.579 |
CLV_Separin_Metazoa | 27 | 31 | PF03568 | 0.421 |
DEG_APCC_DBOX_1 | 311 | 319 | PF00400 | 0.606 |
DEG_APCC_DBOX_1 | 417 | 425 | PF00400 | 0.447 |
DEG_SCF_FBW7_1 | 535 | 540 | PF00400 | 0.697 |
DEG_SPOP_SBC_1 | 128 | 132 | PF00917 | 0.653 |
DEG_SPOP_SBC_1 | 486 | 490 | PF00917 | 0.808 |
DOC_CKS1_1 | 166 | 171 | PF01111 | 0.546 |
DOC_CYCLIN_yClb3_PxF_3 | 236 | 244 | PF00134 | 0.527 |
DOC_MAPK_gen_1 | 460 | 468 | PF00069 | 0.790 |
DOC_MAPK_HePTP_8 | 661 | 673 | PF00069 | 0.320 |
DOC_MAPK_MEF2A_6 | 565 | 573 | PF00069 | 0.495 |
DOC_MAPK_MEF2A_6 | 645 | 653 | PF00069 | 0.405 |
DOC_MAPK_MEF2A_6 | 664 | 673 | PF00069 | 0.190 |
DOC_PP1_RVXF_1 | 153 | 160 | PF00149 | 0.631 |
DOC_PP2B_LxvP_1 | 35 | 38 | PF13499 | 0.638 |
DOC_PP2B_LxvP_1 | 4 | 7 | PF13499 | 0.618 |
DOC_PP2B_LxvP_1 | 687 | 690 | PF13499 | 0.401 |
DOC_PP4_MxPP_1 | 513 | 516 | PF00568 | 0.764 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 530 | 534 | PF00917 | 0.757 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 441 | 446 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 533 | 538 | PF00397 | 0.681 |
LIG_14-3-3_CanoR_1 | 121 | 127 | PF00244 | 0.704 |
LIG_14-3-3_CanoR_1 | 189 | 195 | PF00244 | 0.763 |
LIG_14-3-3_CanoR_1 | 30 | 36 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 303 | 309 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 408 | 414 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 470 | 479 | PF00244 | 0.787 |
LIG_14-3-3_CanoR_1 | 56 | 61 | PF00244 | 0.593 |
LIG_Actin_WH2_2 | 14 | 32 | PF00022 | 0.563 |
LIG_Actin_WH2_2 | 202 | 220 | PF00022 | 0.599 |
LIG_Actin_WH2_2 | 277 | 292 | PF00022 | 0.566 |
LIG_Actin_WH2_2 | 506 | 523 | PF00022 | 0.623 |
LIG_BRCT_BRCA1_1 | 155 | 159 | PF00533 | 0.674 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.424 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.588 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.469 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.619 |
LIG_FHA_1 | 545 | 551 | PF00498 | 0.401 |
LIG_FHA_1 | 593 | 599 | PF00498 | 0.495 |
LIG_FHA_1 | 648 | 654 | PF00498 | 0.414 |
LIG_FHA_1 | 657 | 663 | PF00498 | 0.425 |
LIG_FHA_1 | 703 | 709 | PF00498 | 0.401 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.594 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.437 |
LIG_FHA_2 | 330 | 336 | PF00498 | 0.489 |
LIG_FHA_2 | 360 | 366 | PF00498 | 0.566 |
LIG_FHA_2 | 472 | 478 | PF00498 | 0.785 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.649 |
LIG_FHA_2 | 694 | 700 | PF00498 | 0.401 |
LIG_FHA_2 | 73 | 79 | PF00498 | 0.533 |
LIG_LIR_Apic_2 | 165 | 169 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 263 | 273 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 410 | 421 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 592 | 600 | PF02991 | 0.495 |
LIG_LIR_LC3C_4 | 506 | 510 | PF02991 | 0.632 |
LIG_LIR_LC3C_4 | 567 | 572 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 22 | 28 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 263 | 269 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 538 | 544 | PF02991 | 0.640 |
LIG_LIR_Nem_3 | 588 | 593 | PF02991 | 0.495 |
LIG_PCNA_yPIPBox_3 | 44 | 56 | PF02747 | 0.518 |
LIG_Rb_LxCxE_1 | 135 | 148 | PF01857 | 0.409 |
LIG_SH2_CRK | 430 | 434 | PF00017 | 0.483 |
LIG_SH2_CRK | 553 | 557 | PF00017 | 0.401 |
LIG_SH2_GRB2like | 380 | 383 | PF00017 | 0.395 |
LIG_SH2_PTP2 | 593 | 596 | PF00017 | 0.401 |
LIG_SH2_STAP1 | 88 | 92 | PF00017 | 0.628 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.603 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 449 | 452 | PF00017 | 0.784 |
LIG_SH2_STAT5 | 593 | 596 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 693 | 696 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.627 |
LIG_SH3_1 | 233 | 239 | PF00018 | 0.662 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.682 |
LIG_SH3_3 | 450 | 456 | PF00018 | 0.665 |
LIG_SH3_3 | 480 | 486 | PF00018 | 0.720 |
LIG_SH3_3 | 494 | 500 | PF00018 | 0.761 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.694 |
LIG_SH3_3 | 568 | 574 | PF00018 | 0.401 |
LIG_SH3_3 | 591 | 597 | PF00018 | 0.401 |
LIG_SUMO_SIM_anti_2 | 567 | 573 | PF11976 | 0.495 |
LIG_SUMO_SIM_par_1 | 569 | 576 | PF11976 | 0.495 |
LIG_TRAF2_1 | 564 | 567 | PF00917 | 0.402 |
LIG_WRC_WIRS_1 | 87 | 92 | PF05994 | 0.532 |
LIG_WW_3 | 7 | 11 | PF00397 | 0.780 |
MOD_CDK_SPxxK_3 | 441 | 448 | PF00069 | 0.536 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.621 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.559 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.500 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.671 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.575 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.466 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.703 |
MOD_CK1_1 | 488 | 494 | PF00069 | 0.700 |
MOD_CK1_1 | 533 | 539 | PF00069 | 0.651 |
MOD_CK1_1 | 660 | 666 | PF00069 | 0.383 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.611 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.481 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.647 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.456 |
MOD_CK2_1 | 471 | 477 | PF00069 | 0.782 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.645 |
MOD_CK2_1 | 622 | 628 | PF00069 | 0.401 |
MOD_CK2_1 | 693 | 699 | PF00069 | 0.495 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.525 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.546 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.439 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.654 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.515 |
MOD_GlcNHglycan | 635 | 639 | PF01048 | 0.401 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.791 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.691 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.249 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.577 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.539 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.614 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.578 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.432 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.520 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.782 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.731 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.630 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.608 |
MOD_GSK3_1 | 542 | 549 | PF00069 | 0.553 |
MOD_GSK3_1 | 647 | 654 | PF00069 | 0.425 |
MOD_GSK3_1 | 656 | 663 | PF00069 | 0.382 |
MOD_GSK3_1 | 702 | 709 | PF00069 | 0.401 |
MOD_LATS_1 | 54 | 60 | PF00433 | 0.581 |
MOD_N-GLC_1 | 322 | 327 | PF02516 | 0.569 |
MOD_N-GLC_1 | 657 | 662 | PF02516 | 0.390 |
MOD_N-GLC_1 | 669 | 674 | PF02516 | 0.408 |
MOD_N-GLC_2 | 397 | 399 | PF02516 | 0.634 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.615 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.291 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.671 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.733 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.569 |
MOD_NEK2_1 | 578 | 583 | PF00069 | 0.320 |
MOD_NEK2_1 | 615 | 620 | PF00069 | 0.495 |
MOD_NEK2_1 | 633 | 638 | PF00069 | 0.206 |
MOD_NEK2_2 | 693 | 698 | PF00069 | 0.495 |
MOD_NEK2_2 | 86 | 91 | PF00069 | 0.588 |
MOD_PIKK_1 | 106 | 112 | PF00454 | 0.514 |
MOD_PIKK_1 | 293 | 299 | PF00454 | 0.556 |
MOD_PIKK_1 | 501 | 507 | PF00454 | 0.800 |
MOD_PIKK_1 | 542 | 548 | PF00454 | 0.609 |
MOD_PK_1 | 454 | 460 | PF00069 | 0.778 |
MOD_PKA_1 | 481 | 487 | PF00069 | 0.640 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.747 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.518 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.526 |
MOD_PKA_2 | 407 | 413 | PF00069 | 0.394 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.759 |
MOD_PKA_2 | 622 | 628 | PF00069 | 0.401 |
MOD_PKB_1 | 254 | 262 | PF00069 | 0.607 |
MOD_Plk_1 | 11 | 17 | PF00069 | 0.717 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.570 |
MOD_Plk_1 | 52 | 58 | PF00069 | 0.497 |
MOD_Plk_1 | 537 | 543 | PF00069 | 0.648 |
MOD_Plk_1 | 578 | 584 | PF00069 | 0.342 |
MOD_Plk_1 | 657 | 663 | PF00069 | 0.390 |
MOD_Plk_1 | 669 | 675 | PF00069 | 0.408 |
MOD_Plk_1 | 706 | 712 | PF00069 | 0.606 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.550 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.394 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.471 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.565 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.458 |
MOD_Plk_4 | 515 | 521 | PF00069 | 0.618 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.645 |
MOD_Plk_4 | 589 | 595 | PF00069 | 0.495 |
MOD_Plk_4 | 657 | 663 | PF00069 | 0.320 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.473 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.645 |
MOD_ProDKin_1 | 441 | 447 | PF00069 | 0.528 |
MOD_ProDKin_1 | 533 | 539 | PF00069 | 0.663 |
MOD_SUMO_for_1 | 564 | 567 | PF00179 | 0.495 |
TRG_DiLeu_BaEn_1 | 422 | 427 | PF01217 | 0.555 |
TRG_DiLeu_BaEn_1 | 53 | 58 | PF01217 | 0.609 |
TRG_DiLeu_BaEn_1 | 699 | 704 | PF01217 | 0.495 |
TRG_DiLeu_LyEn_5 | 53 | 58 | PF01217 | 0.609 |
TRG_ENDOCYTIC_2 | 593 | 596 | PF00928 | 0.401 |
TRG_ER_diArg_1 | 244 | 247 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 250 | 253 | PF00400 | 0.658 |
TRG_ER_diArg_1 | 337 | 340 | PF00400 | 0.620 |
TRG_ER_diArg_1 | 469 | 471 | PF00400 | 0.752 |
TRG_ER_diArg_1 | 481 | 483 | PF00400 | 0.731 |
TRG_NES_CRM1_1 | 13 | 27 | PF08389 | 0.639 |
TRG_Pf-PMV_PEXEL_1 | 26 | 31 | PF00026 | 0.603 |
TRG_Pf-PMV_PEXEL_1 | 49 | 53 | PF00026 | 0.432 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P826 | Leptomonas seymouri | 48% | 100% |
A0A3Q8IF57 | Leishmania donovani | 91% | 100% |
E9AGV5 | Leishmania infantum | 92% | 100% |